Ekim Z. Taşkıran

1.5k total citations
70 papers, 739 citations indexed

About

Ekim Z. Taşkıran is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ekim Z. Taşkıran has authored 70 papers receiving a total of 739 indexed citations (citations by other indexed papers that have themselves been cited), including 32 papers in Molecular Biology, 22 papers in Genetics and 13 papers in Surgery. Recurrent topics in Ekim Z. Taşkıran's work include Connective tissue disorders research (5 papers), RNA modifications and cancer (5 papers) and interferon and immune responses (4 papers). Ekim Z. Taşkıran is often cited by papers focused on Connective tissue disorders research (5 papers), RNA modifications and cancer (5 papers) and interferon and immune responses (4 papers). Ekim Z. Taşkıran collaborates with scholars based in Türkiye, United States and Germany. Ekim Z. Taşkıran's co-authors include Mehmet Alikaşifoğlu, Can Koşukçu, Pelin Özlem Şimşek‐Kiper, Koray Boduroğlu, Gülen Eda Ütine, Engin Yılmaz, Ezgi Deniz Batu, Yelda Bilginer, Fatih Özaltın and Özlem Akgün Doğan and has published in prestigious journals such as PLoS ONE, Journal of the American Society of Nephrology and The American Journal of Human Genetics.

In The Last Decade

Ekim Z. Taşkıran

64 papers receiving 731 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ekim Z. Taşkıran Türkiye 15 329 195 169 89 87 70 739
Qingyun Tian United States 17 447 1.4× 67 0.3× 132 0.8× 94 1.1× 68 0.8× 23 1.1k
Pam Speight Canada 18 642 2.0× 86 0.4× 78 0.5× 121 1.4× 110 1.3× 24 1.2k
Carly Selan Australia 15 279 0.8× 88 0.5× 86 0.5× 118 1.3× 29 0.3× 21 674
Bram Piersma Netherlands 7 399 1.2× 64 0.3× 117 0.7× 144 1.6× 145 1.7× 9 1.0k
Olav Klingenberg Norway 18 511 1.6× 89 0.5× 131 0.8× 91 1.0× 77 0.9× 42 900
Takanori Ebisawa Japan 9 1.2k 3.7× 110 0.6× 59 0.3× 69 0.8× 86 1.0× 12 1.5k
Peggy Kirstetter France 12 854 2.6× 83 0.4× 602 3.6× 85 1.0× 69 0.8× 15 1.5k
Youlin Deng China 7 551 1.7× 97 0.5× 53 0.3× 127 1.4× 57 0.7× 12 940
Gabrielle Curinga United States 9 571 1.7× 412 2.1× 98 0.6× 124 1.4× 145 1.7× 11 1.4k
Umut Altunoğlu Türkiye 14 377 1.1× 162 0.8× 46 0.3× 56 0.6× 25 0.3× 54 572

Countries citing papers authored by Ekim Z. Taşkıran

Since Specialization
Citations

This map shows the geographic impact of Ekim Z. Taşkıran's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ekim Z. Taşkıran with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ekim Z. Taşkıran more than expected).

Fields of papers citing papers by Ekim Z. Taşkıran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ekim Z. Taşkıran. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ekim Z. Taşkıran. The network helps show where Ekim Z. Taşkıran may publish in the future.

Co-authorship network of co-authors of Ekim Z. Taşkıran

This figure shows the co-authorship network connecting the top 25 collaborators of Ekim Z. Taşkıran. A scholar is included among the top collaborators of Ekim Z. Taşkıran based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ekim Z. Taşkıran. Ekim Z. Taşkıran is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Orhan, Dıclehan, Şafak Güçer, Pelin Özlem Şimşek‐Kiper, et al.. (2024). AP-1-dependent fibrosis: Exploring its potential role in the pathogenesis of placental transmogrification of the lung (PTL) via tissue-level transcriptome analysis. Pathology - Research and Practice. 258. 155334–155334.
2.
Gültekinoğlu, Merve, Cem Bayram, Ekim Z. Taşkıran, et al.. (2024). Biomedical Efficacy of Garlic‐Extract‐Loaded Core‐Sheath Plasters for Natural Antimicrobial Wound Care. Macromolecular Materials and Engineering. 309(9).
3.
Bayram, Cem, Şükrü Öztürk, Merve Gültekinoğlu, et al.. (2024). Microfluidic Fabrication of Gelatin‐Nano Hydroxyapatite Scaffolds for Enhanced Control of Pore Size Distribution and Osteogenic Differentiation of Dental Pulp Stem Cells. Macromolecular Bioscience. 24(12). e2400279–e2400279. 1 indexed citations
4.
Şimşek‐Kiper, Pelin Özlem, et al.. (2024). Further Expanding the Mutational Spectrum of Gorlin Syndrome in Three Unrelated Families. Molecular Syndromology. 15(3). 175–184. 1 indexed citations
5.
Taşkıran, Ekim Z., et al.. (2023). Mutated Transcripts of ZEB2 Do Not Undergo Nonsense-Mediated Decay in Mowat-Wilson Syndrome. Molecular Syndromology. 14(3). 258–266. 2 indexed citations
6.
7.
Şimşek‐Kiper, Pelin Özlem, et al.. (2023). A novel biallelic CRIPT variant in a patient with short stature, microcephaly, and distinctive facial features. American Journal of Medical Genetics Part A. 191(4). 1119–1127. 5 indexed citations
8.
Taşkıran, Ekim Z., et al.. (2022). Recurrent squamous cell carcinoma and a novel mutation in a patient with xeroderma pigmentosum: a case report. Journal of Medical Case Reports. 16(1). 306–306. 4 indexed citations
9.
Xue, Jingyi, Pelin Özlem Şimşek‐Kiper, Gülen Eda Ütine, et al.. (2021). Expanding the phenotypic spectrum of TNFRSF11A-associated dysosteosclerosis: a case with intracranial extramedullary hematopoiesis. Journal of Human Genetics. 66(6). 607–611. 8 indexed citations
10.
Taşkıran, Ekim Z., Pelin Özlem Şimşek‐Kiper, Eda Ütine, et al.. (2021). Spondyloepimetaphyseal dysplasia EXTL3‐deficient type: Long‐term follow‐up and review of the literature. American Journal of Medical Genetics Part A. 185(10). 3104–3110. 5 indexed citations
11.
Koşukçu, Can, Ekim Z. Taşkıran, Pelin Özlem Şimşek‐Kiper, et al.. (2021). Investigation of Genetic Causes in a Developmental Disorder: Oculoauriculovertebral Spectrum. The Cleft Palate-Craniofacial Journal. 59(9). 1114–1124. 4 indexed citations
12.
Şimşek‐Kiper, Pelin Özlem, Can Koşukçu, Ekim Z. Taşkıran, et al.. (2021). Further expanding the mutational spectrum of brain abnormalities, neurodegeneration, and dysosteosclerosis: A rare disorder with neurologic regression and skeletal features. American Journal of Medical Genetics Part A. 185(6). 1888–1896. 12 indexed citations
13.
López‐Mejías, Raquel, Chiea Chuen Khor, Jong‐Keuk Lee, et al.. (2021). Identification of a shared genetic risk locus for Kawasaki disease and immunoglobulin A vasculitis by a cross-phenotype meta-analysis. Lara D. Veeken. 61(3). 1204–1210. 11 indexed citations
14.
Şimşek‐Kiper, Pelin Özlem, Ekim Z. Taşkıran, Ümüt Arslan, et al.. (2020). Further defining the clinical and molecular spectrum of acromesomelic dysplasia type maroteaux: a Turkish tertiary center experience. Journal of Human Genetics. 66(6). 585–596. 3 indexed citations
15.
Alikaşifoğlu, Ayfer, Nurgün Kandemir, Büşra Aydın, et al.. (2020). Novel insights into diabetes mellitus due to DNAJC3 ‐ defect: Evolution of neurological and endocrine phenotype in the pediatric age group. Pediatric Diabetes. 21(7). 1176–1182. 8 indexed citations
16.
Gönç, E. Nazlı, Ekim Z. Taşkıran, Gülen Eda Ütine, et al.. (2020). Genetic IGF1R defects: new cases expand the spectrum of clinical features. Journal of Endocrinological Investigation. 43(12). 1739–1748. 4 indexed citations
17.
Şekeroğlu, Hande Taylan, Ekim Z. Taşkıran, Pelin Özlem Şimşek‐Kiper, et al.. (2020). Molecular Etiology of Isolated Congenital Cataract Using Next-Generation Sequencing: Single Center Exome Sequencing Data from Turkey. Molecular Syndromology. 11(5-6). 302–308. 6 indexed citations
18.
Ütine, Gülen Eda, Ekim Z. Taşkıran, Can Koşukçu, et al.. (2017). HERC1 mutations in idiopathic intellectual disability. European Journal of Medical Genetics. 60(5). 279–283. 38 indexed citations
19.
Taşkıran, Ekim Z., Emine Korkmaz, Şafak Güçer, et al.. (2014). Mutations in ANKS6 Cause a Nephronophthisis-Like Phenotype with ESRD. Journal of the American Society of Nephrology. 25(8). 1653–1661. 31 indexed citations
20.
Özaltın, Fatih, Ekim Z. Taşkıran, Dilek Ertoy Baydar, et al.. (2011). Disruption of PTPRO Causes Childhood-Onset Nephrotic Syndrome. The American Journal of Human Genetics. 89(1). 139–147. 66 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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